Dataset retrieved from the Finngen database (version 5) including 968 crohn´s cases and 210,300 controls. The dataset has been filtered on variants with P <1e-03.
CD_FINNGEN
A data frame with 29,926rows and 9 variables:
Chromosome, written as for example chr1 or 1
genetic position of the variant
Variant identifier, e.g. rsid
Reference allele
Alternative allele
Standard Error
P-value from Plink run, additive model, reggresion model GLM_FIRTH
Variant effect
variant allele frequency in the UKBB cohort)
CHRONSMALL_968_cases_210300_controls_p_1e-03